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Inhibition and breaking of advanced glycation end-products (AGEs) with bis-2-aminoimidazole derivatives.
Richardson, Mike A; Furlani, Robert E; Podell, Brendan K; Ackart, David F; Haugen, Jessica D; Melander, Roberta J; Melander, Christian; Basaraba, Randall J.
Affiliation
  • Richardson MA; Department of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Forth Collins, CO 80524, USA.
  • Furlani RE; Department of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
  • Podell BK; Department of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Forth Collins, CO 80524, USA.
  • Ackart DF; Department of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Forth Collins, CO 80524, USA.
  • Haugen JD; Department of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Forth Collins, CO 80524, USA.
  • Melander RJ; Department of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
  • Melander C; Department of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
  • Basaraba RJ; Department of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Forth Collins, CO 80524, USA.
Tetrahedron Lett ; 56(23): 3406-3409, 2015.
Article in En | MEDLINE | ID: mdl-26146419
Advanced glycation end-products (AGEs), unregulated modifications to host macromolecules that occur as a result of metabolic dysregulation, play a role in many diabetes related complications, inflammation and aging, and may lead to increased cardiovascular risk. Small molecules that have the ability to inhibit AGE formation, and even break preformed AGEs have enormous therapeutic potential in the treatment of these disease states. We report the screening of a series of 2-aminoimidazloles for anti-AGE activity, and the identification of a bis-2-aminoimidazole lead compound that possesses superior AGE inhibition and breaking activity compared to the known AGE inhibitor aminoguanidine.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tetrahedron Lett Year: 2015 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Tetrahedron Lett Year: 2015 Document type: Article Affiliation country: United States Country of publication: United kingdom